Controlling the macroscopic electrical properties of reduced graphene oxide by nanoscale writing of electronic channels.

The allure of all-carbon electronics stems from the spread of its physical properties across all its allotropes. The scheme also harbours unique challenges, such as tunability of band gap, variability of doping and defect control. Here, we explore the technique of scanning probe tip-induced nanoscale reduction of graphene oxide (GO), which nucleates conducting, [Formula: see text] rich graphitic regions on the insulating GO background. The flexibility of direct writing is supplemented with control over the degree of reduction and tunability of band gap through macroscopic control parameters. The fabricated reduced GO channels and ensuing devices are investigated via spectroscopy and temperature and bias-dependent electrical transport and correlated with spatially resolved electronic properties, using surface potentiometry. The presence of carrier localization effects, induced by the phase-separated [Formula: see text] domains, and large local electric field fluctuations are reflected in the non-linear transport across the channels. Together, the results indicate a complex transport phenomenon, which may be variously dominated by tunnelling or variable range hopping or activated depending on the electronic state of the material.

Interaction of ZnO nanorods with plasmonic metal nanoparticles and semiconductor quantum dots.

We model the enhancement of near band edge emission from ZnO nanorods using plasmonic metal nanoparticles and compare it with emission enhancement from ZnO with semiconducting quantum dots. Selected CdSe quantum dots with absorption energies close to those of Ag and Au nanoparticles are chosen to construct model systems with ZnO to comprehend the role of ZnO's intrinsic defects and plasmonic excitation in realizing the spectrally selective luminescence enhancement. Excitation wavelength dependent photoluminescence spectra along with theoretical models quantifying the related transitions and plasmonic absorption reveal that a complex mechanism of charge transfer between the ZnO nanorods and metal nanoparticles or quantum dots is essential along with an optimal energy band alignment for realizing emission enhancement. The theoretical model presented also provides a direct method of quantifying the relative transition rate constants associated with various electronic transitions in ZnO and their change upon the incorporation of plasmonic nanoparticles. The results indicate that, while the presence of deep level defect states may facilitate the essential charge transfer process between ZnO and the plasmonic nanoparticles, their presence alone does not guarantee UV emission enhancement and strong plasmonic coupling between the two systems. The results offer clues to designing novel multicomponent systems with coupled plasmonic and charge transfer effects for applications in charge localization, energy harvesting, and luminescence enhancement, especially in electrically triggered nanophotonic applications.

Resistive switching in individual ZnO nanorods: delineating the ionic current by photo-stimulation.

Resistive switching in nanostructured metal oxide semiconductors has been broadly understood to originate from the dynamics of its native point defects. Experimental results of switching observed in individual n-ZnO nanorods grown on a p-type polymer is presented along with an empirical model describing the underlying defect dynamics necessary to observe bi-polar switching. Selective photo excitation of electrons into the defect states delineates the incidence and role of an ionic current in the switching behavior. The understanding further extends to the observance of a negative differential resistance regime that is often coincident in such systems. The analysis not only unifies the underlying physics of the two phenomena but also offers further confidence in the proposed mechanism. We conclude by demonstrating that the effective memresistance of such devices is a strong function of the operating bias and identify parameters that optimize switching performance.

Negative photoresponse in ZnO-PEDOT:PSS nanocomposites and photogating effects.

We report negative photoresponse or increase of resistance in nanocomposites of n-type ZnO nanoparticles dispersed in a p-type polymer (PEDOT:PSS) under UV and visible light excitation, contrary to that of planar heterojunctions of the constituents. The underlying mechanism of charge transport, specifically negative photoresponse, is explored using spectroscopic and opto-electrical characterisation. Systemic variability in conductance, photoresponse sensitivity and rate with fractional nanoparticle loading in the nanocomposite is demonstrated. Here, photogenerated electrons in ZnO nanoparticles, trapped by the unbiased interfacial barrier, are understood to localize holes in the PEDOT:PSS conduction channel thereby increasing the overall nanocomposite resistance. Reversibility of the negative PR although with a slow decay rate bears testament to the proposed photogating mechanism as opposed to photocatalytic activity. Replacement of the p-type polymer with an electron transport matrix turns the negative photoresponse positive accentuating the role of the interfacial barrier in tuning the optoelectronic response of the composites. These hybrid materials and their unusual behaviour provide alternative strategies for building devices with novel photogating effects, exploiting the properties of their nanostructured forms.

Spatially resolved photoresponse on individual ZnO nanorods: correlating morphology, defects and conductivity.

Electrically active native point defects have a significant impact on the optical and electrical properties of ZnO nanostructures. Control of defect distribution and a detailed understanding of their physical properties are central to designing ZnO in novel functional forms and architecture, which ultimately decides device performance. Defect control is primarily achieved by either engineering nanostructure morphology by tailoring growth techniques or doping. Here, we report conducting atomic force microscopy studies of spatially resolved photoresponse properties on ZnO nanorod surfaces. The photoresponse for super-band gap, ultraviolet excitations show a direct correlation between surface morphology and photoactivity localization. Additionally, the system exhibits significant photoresponse with sub-bandgap, green illumination; the signature energy associated with the deep level oxygen vacancy states. While the local current-voltage characteristics provide evidence of multiple transport processes and quantifies the photoresponse, the local time-resolved photoresponse data evidences large variations in response times (90 ms-50 s), across the surface of a nanorod. The spatially varied photoconductance and the range in temporal response display a complex interplay of morphology, defects and connectivity that brings about the true colour of these ZnO nanostructures.

EB1 regulates attachment of Ska1 with microtubules by forming extended structures on the microtubule lattice.

Kinetochore couples chromosome movement to dynamic microtubules, a process that is fundamental to mitosis in all eukaryotes but poorly understood. In vertebrates, spindle-kinetochore-associated (Ska1-3) protein complex plays an important role in this process. However, the proteins that stabilize Ska-mediated kinetochore-microtubule attachment remain unknown. Here we show that microtubule plus-end tracking protein EB1 facilitates Ska localization on microtubules in vertebrate cells. EB1 depletion results in a significant reduction of Ska1 recruitment onto microtubules and defects in mitotic chromosome alignment, which is also reflected in computational modelling. Biochemical experiments reveal that EB1 interacts with Ska1, facilitates Ska1-microtubule attachment and together stabilizes microtubules. Structural studies reveal that EB1 either with Ska1 or Ska complex forms extended structures on microtubule lattice. Results indicate that EB1 promotes Ska association with K-fibres and facilitates kinetochore-microtubule attachment. They also implicate that in vertebrates, chromosome coupling to dynamic microtubules could be mediated through EB1-Ska extended structures.

Mathematical model for evaluation of mass transfer limitations in phenol biodegradation by immobilized Pseudomonas putida.

A mathematical model is proposed to analyze the mass transfer limitations in phenol biodegradation using Pseudomonas putida immobilized in calcium alginate. The model takes into account internal and external mass transfer limitations, substrate inhibition kinetics and the dependence of the effective diffusivity of phenol in alginate gel on cell concentration. The model is validated with the experimental data from batch fermentation. The effect of various operating conditions such as initial phenol concentration, initial cell loading, alginate gel loading on the biodegradation of phenol is experimentally demonstrated. Phenol degradation time is found to decrease initially and reach stationary value with increase in cell loading as well as gel loading. The model predicts these trends reasonably well and shows the presence of external mass transfer limitations. A new concept of effectiveness factor is introduced to analyze the overall performance of batch fermentation.